A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3982156



Internal ID18862866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:86498448..86498509hg38UCSC Ensembl
Outerchr1:86964131..86964192hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119701
Supporting Variants
SamplesKWS1
Known GenesCLCA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3982156
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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